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118499-51-7

diphenylmethyl (methyl 3-deoxy-α-D-manno-2-octulopyranosid)onate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118499-51-7 Structure

  • Basic information

    1. Product Name: diphenylmethyl (methyl 3-deoxy-α-D-manno-2-octulopyranosid)onate
    2. Synonyms:
    3. CAS NO:118499-51-7
    4. Molecular Formula:
    5. Molecular Weight: 418.444
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118499-51-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: diphenylmethyl (methyl 3-deoxy-α-D-manno-2-octulopyranosid)onate(CAS DataBase Reference)
    10. NIST Chemistry Reference: diphenylmethyl (methyl 3-deoxy-α-D-manno-2-octulopyranosid)onate(118499-51-7)
    11. EPA Substance Registry System: diphenylmethyl (methyl 3-deoxy-α-D-manno-2-octulopyranosid)onate(118499-51-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 118499-51-7(Hazardous Substances Data)

118499-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118499-51-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,4,9 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118499-51:
(8*1)+(7*1)+(6*8)+(5*4)+(4*9)+(3*9)+(2*5)+(1*1)=157
157 % 10 = 7
So 118499-51-7 is a valid CAS Registry Number.

118499-51-7Relevant articles and documents

SYNTHESIS OF 1,5-LACTONES OF 3-DEOXY-D-manno-2-OCTULOPYRANOSONIC ACID ( KDO)

Auzanneau, France-Isabelle,Charon, Daniel,Szabo, Ladislas,Merienne, Claude

, p. 125 - 136 (2007/10/02)

An unambigous synthesis of methyl 3-deoxy-α-D-manno-2-octulopyranosidono-1,5-lactone from methyl (methyl 3-deoxy-α-D-manno-octulopyranosid)onate via the 7,8-O-isopropylidene derivative is described.Treatment of the 4,5-stannylene derivative of this acetal with benzyl bromide gave the 1,5-lactone from which the protecting groups were removed.The acetylated 1,5-lactone was produced by acetylation of ammonium 3-deoxy-D-manno-2-octulosonate or treatment of the pyridinium salt with dicyclohexylcarbodi-imide and acetylation.No lactone was produced when only HO-7 was unsubstituted.When treated with an excess of 2-methoxypropene, methyl (methyl 3-deoxy-α-D-manno-2-octulopyranosid)onate afforded the 4,5:7,8-di-O-isopropylidene derivative, from which the 7,8-acetal group could be removed selectively.

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